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Publication numberUS3800053 A
Publication typeGrant
Publication dateMar 26, 1974
Filing dateJun 26, 1972
Priority dateJun 26, 1972
Publication numberUS 3800053 A, US 3800053A, US-A-3800053, US3800053 A, US3800053A
InventorsD Lange
Original AssigneeGen Mills Inc
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Process for preparing protein monofilaments
US 3800053 A
Protein monofilaments are prepared from oilseed protein materials and water through the formation of an extrudable plastic mass and the extrusion of same into a gaseous medium. The products find use as food supplements and as texturizing bases for foods such as meat analogs.
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United States Patent m1 Lange Mar. 26, 1974 PROCESS FOR PREPARING PROTEIN MONOFILAMENTS Primary Examiner-A. Louis Monagell Assistant ExaminerJames Robert Hoffman [75] Inventor Dqnald Lange Mmneapohs Attorney, Agent, or FirmAnthony A. Juettner; Gene 0. Enockson [73] Assignees General Mills, Inc., Minneapolis,


22 Filed June 26, 1972 ABSTRACT [21] Appl. No.: 266,200

Protein monofilaments are prepared from oilseed pro- [52] US. Cl 426/364, 42 459, 42 302, tein materials and water through the formation of an 1 264/176 F extrudable plastic mass and the extrusion of same into [51] Int. Cl. A23j 3/00 a gaseous m- Th pr fin e as food sup- [58] Field of Search 99/14, 17; 264/83, 176 F plements and as texturizing bases for foods such as meat analogs. [56] References Cited UNITED STATES PATENTS 6/1954 Boyer 99/14 11 Claims, No Drawings PROCESS FOR PREPARING PROTEIN MONOFILAMENTS This invention relates to a method for preparing protein monofilaments and to the resulting monofilaments. More particularly, it relates to such a method wherein a protein containing plastic mass is prepared and forced while hot through an orifice directly into a gaseous medium to form protein monofilaments.

In recent years a great deal of effort has been expended on the production of texture retaining protein matrices as building blocks for a new series of foods, many of which have been so fabricated to simulate natural cuts of cooked meat, fish, fowl and the like. The early work of Robert A. Boyer as set forth in U.S. Pat. No. 2,682,466 has been extensively followed in this respect. In general, the Boyer process involves the preparation of a spinnable protein dope with subsequent spinning of the dope through a spinnerette into an acid coagulating bath to yield a tow of monofilament fibers. The fibers are caused to set-up or coagulate in the coagulating bath due to the lowering of the pH of the immerging streamlets of the dope to the isoelectric point of the protein. The fibers are oriented by stretching and the pH normally raised somewhat by washing or neutralization. The tow of fibers can then be used through admixture with binders, flavors, fats or oils, coloring agents and the like along with subsequent heat treatments to yield the indicated fabricated foods.

I have now discovered a new, simplified method for preparing protein monofilaments from protein source materials consisting essentially of defatted oil seed proteins having a protein content of at least about 50 percent by weight. Thus I have found that it is only necessary to form a hot plastic mass of the source material with water (with or without certain additives) and extrude such plastic mass through a small orifice or orifices to yield the protein monofilaments. The said monofilaments are new products which retain their textural identity even when added to aqueous liquids. The higher protein content monofilaments which are preferably stretched somewhat can be used to prepare meat analogs as discussed hereinabove with respect to wet spun fibers. They are generally less expensive than the wet spun fibers primarily due to the reduction of the amount of equipment required i.e., no coagulating or set baths are required. Where comparable monofilament diameters are obtained, the monofilaments of my invention can serve as reasonably acceptable replacements for the wet spun fibers in the said meat analog preparations. The flavor characteristics of meat analogs prepared from the fibers of the present invention hold up better in retorting than the prior practices. Especially where the monofilaments of the invention have lower protein contents, they are readily broken into short lengths yielding a new form of protein additive for supplementing a variety of foods.

As indicated, the protein source material consists essentially of defatted oilseed proteins having a protein content of at least about percent by weight. Of the oilseeds, soy protein materials are preferred due to their ready availability and functional properties. Other oilseed proteins such as rapeseed, cottonseed, peanut and sesame seed can be used. The oilseeds can be in the form of defatted flours, concentrates of increased protein content over the flours and isolates wherein most of the non-protein materials have been removed. The

higher the protein content, the higher the strength in the new monofilaments. Thus where the protein content of the source material is above about percent, i.e., 70 to percent, by weight the monofilaments can be stretched and oriented and have good strength. Protein contents of less than about 70 percent by weight but within the recited range yield fibers which can readily be broken into short lengths. Such short-break fibers do, however, retain their structural and textural identity when placed in aqueous liquids.

Mixtures of the oilseed source materials can be used in the present invention. Thus, isolates can be mixed with flours and/or concentrates and the various oilseed materials can be used in combination with each other. Additionally, the oilseed source materials can be used in combination with other functional proteins, such as gluten, rennet casein and the like so long as such other protein materials do not alter the characteristics of the monofilaments to the extent that they can no longer be termed oilseed protein based monofilaments. The protein materials must be functional-that is, not heat or otherwise denatured so as to become relatively inactive.

The oilseed protein source material is mixed with water and heated to form the extrudable plastic mass. The amount of water can vary over relatively wide limits and optimally will generally be different for each protein source material or mixture of protein source materials. The water content needed to form the plastic mass will preferably fall within about 25-60 percent by weight based on the total composition of the extrudable plastic mass. In many instances, the water content will be in the especially preferred range of about 35 to 50 percent by weight of the total composition.

It was indeed surprising to find that protein monofilaments could be obtained from the protein source material and water alone in accordance with the process of the invention which requires no after-treatment. Also, surprisingly, the monofilaments can be obtained over a relatively broad pH range, with the properties of the monofilaments being tailored somewhat dependent on the pH used. Water soluble acids and bases can be added to alter the pH of the extrudable plastic mass and thence alter the pH and properties of the monofilaments. Of the water soluble acids, hydrochloric, acetic, citric and phosphoric are preferred. Of the water soluble bases, sodium and ammonium hydroxides are preferred. The pH can preferably vary from about 2.0 to 10 5, with the especially preferred range being from about 4.0 to 9.0. Monofilaments produced in the acid pH range generally show somewhat greater strength characteristics and thus are somewhat preferred.

Other additives can also be included in the extrudable plastic masses. In this respect, extrusion aids can be added to improve the extrudability of the compositions. Such materials can be organic or inorganic reducing agents, with the latter being preferred-Le, the alkali metal and ammonium sulfites and bisulfites such as sodium sulfite. Plasticizers for the monofilaments can also be included. A preferred material is glycerol.

Additionally, my process makes it possible to incorporate flavors, colors, vitamins and the like internally in the monofilaments simply by including them in the extrudable plastic masses.

The oilseed protein source material, water and optional additives are mixed and heated until a relatively homogenous plastic mass is obtained. The plastic mass is preferably obtained at temperatures in the range of about 175 to 300 F., it being understood that the optimum temperature for each such plastic mass will depend somewhat on the particular protein source mate- 5 rial employed, the water-protein source material ratio and the presence or absence of the optional additives. Temperatures in the upper part of the range tend to give monofilaments of increased strength. An especially preferred range for most of the plastic masses is from about l90-285 F. The extrusion temperatures are below the point where the exiting monofilaments would puff to any appreciable extent. The materials can desirably be pre-mixed and then charged to an extruder equipped with heating and mixing means. A val5 riety of such extruders are readily available commercially. Where the heating takes place in the extruder, the plastic mass will also be formed in the extruder. The extruder pressure is not critical, it being only necessary that sufficient pressure be employed to aid in the formation of and/or maintain the heated mass in a plastic state and then force the said plastic mass out of the extruder orifice or orifices to yield the protein monofilaments. As indicated above, the orifice or orifices will have a cross section or diameter of less than about 50 mils n e m rsprqfs ably be b ut 1.0. n (i.e., 2-10 mils) where the object is to obtain monofilaments for use in meat analog preparations.

The monofilaments form almost instantaneously as they exit from the extruder orifice into a gaseous atmosphere. Air is entirely suitable as the gaseous atmosphere simply as a matter of economic practicality. Of course other essentially inert gases such as nitrogen and the like can be used if desired.

The monofilaments prepared from the higher protein content source materials are desirably stretched somewhat as they leave the extruder. The stretching reduces the diameter of the monofilaments and tends to orient the protein molecules therein.

The monofilaments of the invention are new texturizing building blocks for foods and/or serve as protein supplements to foods. In the former respect, they can be mixed with binders, flavors, coloring agents and the like to yield fibrous products generally simulating natural cooked meat, fish or fowl portions. The short-break fibers can be used as external additives to ready-to-eat cereals, for example, to increase the protein content of such cereals or to maintain the over-all protein content thereof when the same are sugar coated.

The following examples serve to illustrate certain preferred embodiments of the invention without being limiting. In all of the examples the monofilaments were extruded into air at ambient room temperature.

EXAMPLE I A protein containing mix was made up as follows:

Soy isolate (Promine D, I000 gm. 80% by weight protein) Water 660 ml. Na,so, 10 gm. Glycerine 330 ml. Nl-LOH-IS N. ml.

The above ingredients were mixed (pH-=) and then fed into a Wayne extruder equipped with a heater and a die having an 8 mil diameter circular die opening. The auger rotation was held at 34 rpm and the extrusion temperature was varied from 200 to 295 F. At 200 F. the monofilament was relatively weak and, as

EXAMPLE Il Example I was essentially repeated except using a 10 mil die opening, a temperature of 275-285 F. and protein mix having a pH of 4.0 made up of the following ingredients:

Promine D 500 gm. Water 255 ml. 12 N. HCl 34.5 ml. Glycerine gm. Na,SO 5 gm.

There was obtained an off-white monofilament strand which was termed very strong.

EXAMPLE Ill Example II was essentially repeated using the following mixes tailored to have different pH s:

A B C Prominc D 500 gm. 500 gm. 500 gm. Water 220 ml. 220 ml. 233 ml. NH OH l5 l3 ml. N.

HCI 12 N. 13.75 mi. Glycerine 165 gm. 165 gm. 165 gm. Na SO, 5 gm. 5 gm. 5 gm.

The extrusion mixes had pHs of 9.4, 7.6 and 6.0, respectively. The pH 6.0 monofilaments were slightly stronger than those prepared from mixes A and B. However, all of the monofilaments had reasonable strength. The monofilaments from Examples II and III were tested for rehydration characteristics by soaking 10 gm. of the monofilaments in cold tap water for 5 minutes, draining on a screen for 5 minutes and then reweighing. Results were as follows:

Monofilaments of Example Rehydrated Weight (average of two This data indicates that the monofilaments prepared from alkaline pH mixes have higher water take-up than the monofilaments from acidic pH mixes.

EXAMPLE IV Example III, C was essentially repeated except that the glycerine was reduced by 50 percent and also completely eliminated. Good monofilaments were obtained in both runs, the same being a little less pliable than monofilaments made from glycerine containing formulations.

EXAMPLE V Example 111, C was essentially repeated except that the HCl in the mixes was replaced with 14 gm. citric acid, ml. 85 percent phosphoric acid and ml. 99.7 percent acetic acid, respectively. Good monofilaments were obtained in all three instances.

EXAMPLE VI Extrusion mixes were prepared from soy isolate (Promine FS 90-93 percent by weight protein) and water using 1,000 gm. isolate, 705 ml. water and additions of 70 ml. conc. HCl, 15 ml. cone. HCl, no acid or base addition and ml. 44 percent by weight aqueous sodium hydroxide, respectively. The mixes were extruded as in the previous Examples at rpm through a die containing 3 mil openings (die temperature of 250-80 F.). The resulting monofilaments having pH values of 3.5, 6.2, 7.2 and 8.8, respecitvely, varied in diameter from 4.7 to 6.3 mils. The tensile strengths of the fibers were all very good and increased as the pH increased. Water uptake also increased with increasing pH whereas the wet shear characteristics decreased.

EXAMPLE VII The following extrusion mixes were prepared and extruded as in Example II:

Good monofllaments were obtained. The monofilaments of D were not as strong as the others but had a higher water uptake. The monofilaments of B were slightly stronger than those of A and C and also had a' somewhat better water uptake.

EXAMPLE Vlll Example VII, was essentially repeated except that the following extrusion mixes were used:

A B C Promine D 400 gm. 400 gm.- 400 gm. Gluten 100 gm. Lactalbumin 100 gm. Rennet casein 100 gm. Water 235 ml. 235 ml. 235 m1. HCl 12 N. 14 ml. 14 ml. 14 ml. Na SO 5 gm. 5 gm. 5 gm.

All of the resulting extrudable plastic masses produced long continuous monofilaments having reasonably good strength.

EXAMPLE IX A mix was made up as follows:

Defatted soy flour (55% 500 gm. by weight protein) Water 285 ml. HCl cone. 5 ml.

The mix (pH 6.2) was formed into a plastic mass and extruded similarly as in Example 11 (25 rpm, die temperature of 250 F., die openings were 3.5 mils). The monofilaments were fairly weak and broke readily into shorter lengths.

EXAMPLE X The following extrusion mixes were prepared:

Cottonseed 500 gm. protein concentrate (66.3% by weight protein) Sesame seed flour (47.0% by weight protein) Rapeseed protein concentrate (62% by weight protein) Water ml. 250 m1. 500 ml.

Monofilaments of textural integrity were obtained in all instances when the mixes were extruded similarly as in Example IX. The strength was lower than when using an isolate such as soy isolate of higher protein content.

EXAMPLE X1 An extrusion mix was prepared from:

Soy isolate 1000 gm. Water 650 ml. Conc. HCl 15 ml. Dry beef flavor 25 gm.

The mix when extruded similarly as in Example 1X yielded monofilaments having a beefy flavor. Correspondingly, other flavors such as almond, coconut, lime, orange, walnut and the like have been incorporated into the extrusion mixes to yield flavored fibers.

EXAMPLE XII The monofilaments prepared in Example V] were used to prepare ham analogs using the formula:

The ingredients were mixed and heated at l80l 85 F.

under a pressure of about 8 psig. for 4% minutes to yield ham flavored analogs (the pH of each mix was adjusted to about 5.5 to 6.1 by the addition of citric acid or sodium bicarbonate). The analogs prepared from the monofilaments having a pH of 6.2 or 7.2 had the overall best eating quality. The analog from the 8.8 pH monofilaments was softer but more moist whereas the analog from the pH 3.5 monofilaments was slightly grainy.

The embodiments of the invention in which an exclusive property is claimed are defined as follows:

1. The process of preparing protein monofilaments which comprises mixing a protein source material consisting essentially of defatted oilseed protein materials having a protein content of at least about 50 percent by weight with water wherein the water is present in an amountof about 25 to 60 percent by weight of the total composition, heating the mixture to form an essentially homogeneous, extrudable, plastic mass having a pH in the range of about 2.0 to 10.5, and extruding the hot plastic mass through an orifice or a multiplicity of orifices having a diameter of less than 50 mils directly into an essentially inert gaseous medium to yield the protein monofilaments.

2. The process of claim 1 wherein the oilseed protein material has a protein content of about 50 to percent by weight.

3. The process of claim 1 wherein the oilseed protein material has a protein content of about 70 to percent by weight.

4. The process of claim 1 wherein the water content of the composition is about 35 to 50 percent by weight.

5. The process of claim 1 wherein the plastic mass has a pH of about 4.0 to 9.0.

6. The process of claim 1 wherein the plastic mass also contains an extrusion aid and a plasticizer.

7. The process of claim 6 wherein the extrusion aid is sodium sulfite and the plasticizer is glycerine.

8. The process of claim 1 wherein the plastic mass also contains a flavoring agent.

9. The process of claim 1 wherein the extrusion is carried out at a temperature of about to 300 F.

10. The process of claim 1 where the orifice diameter is from about 2 to 10 mils.

11. The process of claim 1 wherein the gaseous medium is air.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US2682466 *May 6, 1952Jun 29, 1954Robert A BoyerHigh protein food product and process for its preparation
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3953612 *Jan 6, 1975Apr 27, 1976Miles Laboratories, Inc.Extrusion through spinneret
US3984576 *Sep 9, 1974Oct 5, 1976The Quaker Oats CompanyMeatless marbled, semi-moist pet food
US4017646 *Dec 11, 1975Apr 12, 1977Ralston Purina CompanyProcess for producing pH modified protein filaments
US4029823 *Jun 12, 1974Jun 14, 1977The Quaker Oats CompanyMethod of making a dry pet food having a marbled meat-like texture
US4039691 *Dec 31, 1975Aug 2, 1977Campbell Soup CompanyProtein texturization by extrusion with internal steam injection
US4095001 *Dec 31, 1975Jun 13, 1978Campbell Soup CompanySoybeans, extrusion
US4103034 *Oct 18, 1974Jul 25, 1978Nabisco, Inc.Process for production of textured protein flakes
US4118520 *Mar 9, 1977Oct 3, 1978Thomas J. Lipton, Inc.Protein fibres
US4139648 *Oct 31, 1977Feb 13, 1979Campbell Soup CompanyProtein texturization
US4156028 *Mar 3, 1977May 22, 1979Societe D'assistance Technique Pour Produits Nestle S.A.Process for producing proteinic filaments of high nutritive value
US4207349 *Feb 17, 1978Jun 10, 1980Thomas J. Lipton, Inc.Edible milk solids in snacks
US4208436 *Aug 1, 1978Jun 17, 1980Thomas J. Lipton, Inc.Meat analogues containing dry spun protein fibers
US4245552 *Sep 29, 1978Jan 20, 1981Campbell Soup CompanyProtein texturization
US4276319 *Jan 17, 1979Jun 30, 1981Ralston Purina CompanyProcess for the production of a granulated protein gel suitable as a meat extender
US4612203 *Oct 31, 1984Sep 16, 1986The Procter & Gamble CompanyAcidified meat analog products
US4615899 *Dec 10, 1984Oct 7, 1986The Procter & Gamble Co.Sauce containing acidified textured protein
EP0146510A1 *Oct 12, 1984Jun 26, 1985Aga AktiebolagMethod of extrusion
WO1996017981A1 *Nov 28, 1995Jun 13, 1996Du PontProcess for producing zein fibers
WO2012158023A1 *May 10, 2012Nov 22, 2012Ojah B.V.Method of making structured protein compositions
U.S. Classification426/656, 264/211.14, 426/802, 426/506, 426/459, 264/211.11
International ClassificationD01F4/00, A23J3/26, A23J3/22, A23J3/00
Cooperative ClassificationA23J3/227, A23J3/26, Y10S426/802
European ClassificationA23J3/26, A23J3/22C2